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FIGURE 5 in Positive allometry for exaggerated structures in the ceratopsian dinosaur Protoceratops andrewsi supports socio-sexual signaling
FIGURE 5. Life restoration of adult Protoceratops andrewsi (foreground) engaging in speculative display postures, an activity in which non-mature animals (background) do not take part. Artwork by Rebecca Gelernter, who retains the copyright on this image — used with permission.
FIGURE 4 in Positive allometry for exaggerated structures in the ceratopsian dinosaur Protoceratops andrewsi supports socio-sexual signaling
FIGURE 4. Allometric relationships for frill length (1), frill width (2) and the width across the jugal bosses (3). Solid lines show the fitted lines from SMA regression, dashed grey lines show the line of isometry (slope = 1 and intercept = 0). All measurements were originally in mm prior to log transformation.
FIGURE 5. The skull, NFL 2074 in A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position
FIGURE 5. The skull, NFL 2074, referred specimen of Numataphocoena yamashitai in anterior view. 1, photo, 2, line art.
FIGURE 4. The skull, NFL 2074 in A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position
FIGURE 4. The skull, NFL 2074, referred specimen of Numataphocoena yamashitai in lateral view. 1, photo, 2, line art.
FIGURE 6 in A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position
FIGURE 6. Life restoration of Numataphocoena yamashitai. Art work by Tatsuya Shinmura (Ashoro Museum of Paleontology).
FIGURE 8 in A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position
FIGURE 8. The maxillary terrace from the posterior dorsal infraorbital foramen on the maxilla. 1 and 2, NFL 7, the type of Numataphocoena yamashitai. 3 and 4, NFL 2074, the referred specimen.
FIGURE 3. The skull, NFL 2074 in A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position
FIGURE 3. The skull, NFL 2074, referred specimen of Numataphocoena yamashitai in ventral view. 1, photo, 2, line art.
FIGURE 2. The skull, NFL 2074 in A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position
FIGURE 2. The skull, NFL 2074, referred specimen of Numataphocoena yamashitai in dorsal view. 1, photo, 2, line art.
FIGURE 1. 1 in A new skull of the fossil porpoise Numataphocoena yamashitai (Cetacea: Phocoenidae) from the upper part of the Horokaoshirarika Formation (lower Pliocene), Numata Town, Hokkaido, Japan, and its phylogenetic position
FIGURE 1. 1, Locality maps, 2, stratigraphic sections of the locality based on previous studies which are mentioned in the text. This figure is modified from Tanaka (2016).
Fig. 4 Primers binding position distributed along the 1,500 in Same information, new applications: revisiting primers for the avian COI gene and improving DNA barcoding identification
Fig. 4 Primers binding position distributed along the 1,500 bp of the avian COI gene. A Binding position of forward primers. B Binding position of reverse primers
Fig. 3 in Basicranial morphology and phylogenetic position of the upper Eocene carnivoramorphan Quercygale
Fig. 3. Systematic position of Quercygale. Strict consensus of 12 most parsimonious trees; heuristic search—100 random addition sequence iterations; tree length 386 steps; consistency index = 0.339, retention index = 0.657, rescaled consistency index 0.223. Bremer support values for each ingroup node are labeled.
Fig. 2 in Basicranial morphology and phylogenetic position of the upper Eocene carnivoramorphan Quercygale
Fig. 2. Quercygale angustidens, upper Eocene, Quercy area, France, NRM−PZ M2329. Ventral lateral view of the right auditory region. A. Stereophoto. B. Explanatory drawing of the same. Anterior is to the top.
Supplemental data for: Evaluation of SARS-CoV-2 response at the University of North Carolina (UNC) at Charlotte using percent positivity data and viral genomic sequence data.
<p>Supplemental data for:</p> <p>Evaluation of SARS-CoV-2 response at the<br>University of North Carolina (UNC) at Charlotte<br>using percent positivity data and viral genomic<br>sequence data.</p> <p>Submitted to Biocarla 2024</p> <p>https://carla2024.org/portfolios/biocarla/</p> <p>Authors:</p> <p>Daniel Janies 1,2,3 [0000−0002−7890−9906], Shirish Yasa 1,2,3 [0000−0003−3217−4921],<br>Colby T. Ford 1,3,4 [0000−0002−7859−3622] Jannatul Ferdous 2,3 [0000−0003−3053−9616],<br>William Taylor 2,3 [0009−0000−6204−1172], April Harris 2,3 [0009−0009−2557−7926],<br>Sam Kunkleman 2,3 [0000−0002−2309−6418], Juan Bolanos 2,3, Kevin Lambirth 2,3 [0000-0002-6568-543X], Denis<br>Jacob Machado 1,2,3 [0000−0001−9858−4515], Cynthia Gibas 1,2,3 [0000−0002−1288−9543],<br>and Jessica Schlueter 1,2,3 [0000−0002−6490−0580]</p> <p>Affiliations:</p> <p>1) Center for Computational Intelligence to Predict Health and Environmental Risks<br>(CIPHER), University of North Carolina at Charlotte 28223, USA<br>Correspondence to: djanies@charlotte.edu<br>https://cipher.charlotte.edu<br>2) Department of Bioinformatics and Genomics, University of North Carolina at<br>Charlotte 28223, USA https://cci.charlotte.edu/departments/<br>department-of-bioinformatics-and-genomics/<br>3) College of Computing and Informatics, University of North Carolina at Charlotte<br>28223, USA https://cci.charlotte.edu<br>4) School of Data Science, University of North Carolina at Charlotte 28223, USA<br>https://sds.charlotte.edu<br>5) Division of Research, University of North Carolina at Charlotte 28223, USA<br>https://research.charlotte.edu/</p> <p> </p>
FIG. 1 in Position taxonomique de Hemiperis micrantha (Frapp. ex Cordem.) Schltr. (Orchidaceae; Orchidoideae; Habenariinae), par séquençage des gènes ITS et matK
FIG. 1. — Arbre phylogénétique à maximum de vraisemblance déduit de l'analyse matK (A) et ITS (B). La prise en charge du bootstrap à partir des analyses du maximum de vraisemblance (MV) supérieures à 50% est indiquée au-dessus des branches. Le symbole (*) représente les espèces types des genres Cynorkis Thouars et Benthamia A. Rich. et le symbole (+) positionne Cynorkis micrantha (Frapp. ex Cordem.) Schltr. dans les arbres.
FIG. 3 in Position taxonomique de Hemiperis micrantha (Frapp. ex Cordem.) Schltr. (Orchidaceae; Orchidoideae; Habenariinae), par séquençage des gènes ITS et matK
FIG. 3. — Cynorkis micrantha (Frapp. ex Cordem.) Schltr. photographié in situ (photographies de Frédéric Henze): A, fleur vue de face; B, fleur vue de profil; C, inflorescence; D, feuille.
Fig. 4. A. Strict consensus trees for 8638 trees 413 in Phylogenetic position of the crocodylian Megadontosuchus arduini and tomistomine palaeobiogeography
Fig. 4. A. Strict consensus trees for 8638 trees 413 steps long derived from the analysis including Megadontosuchus arduini. The geographic range of tomistomines is abbreviated as follows: CE, Central Europe; EA, Eastern Asia; NA, North America; NAf, Northern Africa; SEA, South Eastern Asia; WE, Western Europe; NWE, North Western Europe. Consensus statistics: tree length (L) = 430; consistency index (CI) = 0.4581; homoplasy index (HI) = 0.5419; CI excluding uninformative characters = 0.4261; HI excluding uninformative characters = 0.5739; retention index (RI) = 0.7272; rescaled consistency index (RC) = 0.3331. B. Strict consensus topology for 4344 trees 409 steps long derived from the analysis excluding M. arduini. Consensus statisics: L = 416; CI = 0.4712; HI = 0.5288; CI excluding uninformative characters = 0.4388; HI excluding uninformative characters = 0.5612; RI = 0.7406; RC = 0.3489. C. Adams consensus tree derived from the 47 taxa matrix.
Fig. 3 in Phylogenetic position of the crocodylian Megadontosuchus arduini and tomistomine palaeobiogeography
Fig. 3. Tomistomine crocodile Megadontosuchus arduini (de Zigno, 1880), MGPD 1Z, lectotype from Monte Duello (Roncà, Province of Verona, NE Italy); middle Eocene. Skull in occipital view. Photograph (A) and explanatory drawing of the same (B).
Fig. 1 in Phylogenetic position of the crocodylian Megadontosuchus arduini and tomistomine palaeobiogeography
Fig. 1.Tomistomine crocodile Megadontosuchus arduini (de Zigno, 1880), MGPD 1Z, lectotype from Monte Duello (Roncà, Province of Verona, NE Italy); middle Eocene. Skull in dorsal view. Photograph (A) and explanatory drawing of the same (B).
Fig. 5 in Phylogenetic position of the crocodylian Megadontosuchus arduini and tomistomine palaeobiogeography
Fig. 5. Schematic global distribution of tomistomine fossil record and approximate present range (in thick circle) of the only extant species Tomistoma schlegelii. Taxa are reported from the literature without taxonomic changes. Abbreviations: C., Charactosuchus; D., Dollosuchus; F., Ferganosuchus; G., Gavialosuchus; K., Kentisuchus; M., Megadontosuchus; Ma., Maroccosuchus; P., Paratomistoma; R., Ramphosuchus; T., Tomistoma; Th., Thecachampsa; e., early; m., middle; l., late.
Fig. 2 in Phylogenetic position of the crocodylian Megadontosuchus arduini and tomistomine palaeobiogeography
Fig. 2. Tomistomine crocodile Megadontosuchus arduini (de Zigno, 1880), MGPD 1Z, lectotype from Monte Duello (Roncà, Province of Verona, NE Italy); middle Eocene. Skull in ventral view. Photograph (A) and explanatory drawing of the same (B).
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.